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HRID 41674作成日:2026年10月25日

Hexane → 3-Bromo-5-(4-chlorophenyl)-2-ethyl-thiophene

https://huagongshe.com/reaction/41674

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Trimethyl borateHCID 8470—
反応物Sodium CarbonateHCID 10340—
反応物TriphenylphosphineHCID 11776—
反応物1-Chloro-4-iodobenzeneHCID 12510—
反応物3,5-Dibromo-2-ethylthiopheneHCID 13177178—
反応物ButyllithiumHCID 178418339—
触媒palladium(II) acetateHCID 167845—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Bromo-5-(4-chlorophenyl)-2-ethyl-thiopheneHCID 5958464575%

反応条件

温度-78 °C

反応手順

To a solution of 3,5-dibromo-2-ethyl-thiophene (3.28 g, 12.15 mmol) in diethyl ether (50 ml) at −78° C. under N2 is added, slowly, 2.5M butyl lithium in hexane solution (4.86 ml, 12.15 mmol) over 10 minutes and the reaction stirred at −78° C. for a further 30 minutes. The reaction is then cooled to −78° C. before the dropwise addition of trimethyl borate (1.64 ml, 14.6 mmol) over 5 minutes. The reaction is stirred at −78° C. for 30 minutes, then allowed to warm to room temperature and stirred for a further 60 minutes. Palladium acetate (68 mg, 0.3 mmol), triphenylphosphine (314 mg, 1.2 mmol) and 4-chloro-iodobenzene (4.9 g, 12.15 mmol) is then added to the reaction, followed by THF (50 ml) and 1N sodium carbonate solution (20 ml) and the reaction is heated to reflux for 3 hours. The cooled reaction mixture is partitioned between ether (250 ml) and water (300 ml). The organic layer is separated, dried over magnesium sulphate, filtered and evaporated under reduced pressure. The residue is therefore purified by flash chromatography on silica gel to give 3-bromo-5-(4-chlorophenyl)-2-ethyl-thiophene as a white solid (2.75 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530667B2
出典データセットuspto-grants-2013_09
ORD IDord-f69b0b8d89b34c5cb08116bccd469b1f
出典メモuspto-grants-2013_09